Validation Manager Associate

QA Validation Associate - Cork, Ireland - 12 Months Contract Are you interested in joining a world leading biopharmaceutical company, focused on developing advanced and innovative treatments for those suffering with rare diseases?This is a fantastic opportunity to work in a state-of-the-art facility in Cork.You will be joining a leading Biopharmaceutical...

Are you looking for a Validation role with a dynamic Medical Device company? Then we have the role for you.Note: no sponsorship is provided for this role, a Stamp 1G or Stamp 4 is required.Key Responsibilities:Prepare software validation protocols and execute these protocols, ensuring sign-off is obtained at each stage.Prepare software design specifications...

About the PositionWe are looking for an experienced QA Validation Associate to oversee the implementation of new manufacturing processes, equipment, computer systems, laboratory systems and changes to existing equipment. This is a 12-month contract role.

About Blackfield AssociatesAt Blackfield Associates, we strive to provide innovative recruitment solutions to the pharmaceutical industry. We take pride in matching talented professionals with leading companies, fostering growth and excellence.About the Role:This position requires a deep understanding of process validation regulations and a proven track...

We're currently recruiting for an exciting opportunity with an award-winning Medical Device organization based in Cork.This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.DutiesEnsure validation activities completed comply with US and EU regulations, GBSC procedures and EHS...

About the RoleWe're seeking a talented Process Validation Engineer to join our client's team. The ideal candidate will have in-depth knowledge of 21 CFR 820, 21 CFR 11, ISO 13485, and European regulations associated with the medical device industry.Assist in development of sampling plans, test plans, and data analysis related to process validation.The role...

Elusav Recruitment have an amazing opportunity for a CQV Engineer with a leading global biopharma company in Waterford, Ireland.As the CQV Engineer, you will be required to support new product introductions, equipment qualification and the site requalification program.Responsibilities:Designing, executing and reporting on PV/Process Performance...

About Blackfield AssociatesAt Blackfield Associates, we pride ourselves on delivering exceptional recruitment services to the pharmaceutical industry. Our goal is to connect talented professionals with leading companies, driving innovation and growth.About the Job:This role involves working closely with the production team to ensure equipment, systems, and...

**About the Role:**We are seeking a skilled QA Validation Associate to join our team at Quanta Consultancy Services Ltd.**Key Responsibilities:Work closely with the QAV team to ensure smooth project executionConduct QA oversight on various aspects of our operations, including HVAC/Utilities qualification, equipment qualification, and cleaning...

1 day ago Be among the first 25 applicantsDirect message the job poster from Recruitment by AphexRecruitment Lead | C&Q | Validation | Quality | Life Sciences Talent SpecialistOur Team:In the Validation Engineer role, you will be required to support new product introductions, equipment qualification and the site requalification program. The Validation...

Job DescriptionElusav Recruitment is seeking a highly skilled CQV Engineer to join a leading global biopharma company in Waterford, Ireland.The successful candidate will be responsible for supporting new product introductions, equipment qualification, and the site requalification program.Main ResponsibilitiesDesigning, executing, and reporting on PV/Process...

We are looking for a talented CQV Engineer to join our client's team in Waterford, Ireland.The successful candidate will be responsible for supporting new product introductions, equipment qualification, and the site requalification program.Main ResponsibilitiesThe CQV Engineer will be responsible for:Designing, executing, and reporting on PV/Process...

Job SummaryLife Science Recruitment is currently recruiting for a Process Validation Engineer to join an award-winning Medical Device organization based in Cork. This is an exciting opportunity for anyone looking to join a leading multinational company that is one of the best at what they do.This position involves ensuring validation activities comply with...

Job Description">Provide project management oversight from a Quality perspective for FUE activities related to products and facilities, utilities, equipment (FUE).">We are seeking a highly skilled QA Validation Associate to join our team at Claran Consultants Ltd. As a key member of our team, you will be responsible for the review and approval of validation...

Job Description: Computer Systems Quality Assurance RoleThis role supports the expansion of Enterprise Resource Planning Systems and associated applications to new and existing manufacturing sites. The successful candidate will deliver quality oversight to ensure assigned systems meet corporate Computer System Validation standards.The ideal candidate will...

About the RoleWe are seeking a highly skilled CQV Engineer to join our client's team in Ireland.The successful candidate will be responsible for supporting new product introductions, equipment qualification, and the site requalification program.Main ResponsibilitiesDesigning, executing, and reporting on PV/Process Performance Qualifications.Designing,...

Associate Manager, AdditiveLocation: Stryker Anngrove, CarrigtwohillReporting to: Engineering ManagerAre you ready to step into a leadership role and drive innovative technologies in the medical field? We are seeking a motivated and collaborative Associate Manager to lead and support our New Product Introduction (NPI) programs within the Joint Replacement...

OverviewThe PM Group's Outsourced Technical Services (OTS) Department partners with global leaders across various industries to find the best candidates for their current and ongoing business needs.We are seeking a skilled and experienced QA Validation Specialist to join a Client Validation team in a GMP regulated environment. The selected candidate will be...

About This OpportunityWe are seeking a talented Senior Staff Quality Validation Engineer to join our team and contribute to the development of our validation strategy.Key Accountabilities:Developing and implementing validation strategies aligned with regulatory requirements.Collaborating with local teams to define best practices and provide technical...

OverviewThe Outsourced Technical Services (OTS) Department at PM Group partners with Global leaders across a range of industries to find the best people for their current and ongoing business needs. Partnering with PM Group and our clients means that you will gain unrivalled experience working with global brands.We are seeking a skilled and experiencedQA...